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Alessandra Franzoni

Showing results (11-20 of 34) with videos related to

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British Journal of Haematology|September 10, 2009
Unexpected phenotype of a typical NPM1 mutantAnnalisa Pianta, Dora Fabbro, Daniela Damiani, et al.
Endocrine|November 8, 2022
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structureAlessandra Franzoni, Federica Baldan, Nadia Passon, et al.
Neuropediatrics|October 10, 2017
Neurovisual Assessment in Children with Ataxia TelangiectasiaAlessandro Iodice, Jessica Galli, Anna Molinaro, et al.
Frontiers in Human Neuroscience|March 21, 2022
Age-Related Effects on the Spectrum of Cerebral Visual Impairment in Children With Cerebral PalsyJessica Galli, Erika Loi, Anna Molinaro, et al.
Clinical Case Reports|October 20, 2025
A Prenatal Diagnosis of Verheij Syndrome in a Fetus Harboring a de novo <i>PUF60</i> VariantCatia Mio, Maria Orsaria, Alessandra Franzoni, et al.
American Journal of Hematology|June 14, 2013
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patientsDaniela Damiani, Mario Tiribelli, Alessandra Franzoni, et al.
BMC Medical Genetics|October 15, 2015
A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosisPatrizia Dello Russo, Alessandra Franzoni, Federica Baldan, et al.
European Journal of Human Genetics : EJHG|November 12, 2020
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotypeCatia Mio, Lorenzo Allegri, Nadia Passon, et al.
Endocrine Pathology|January 25, 2011
Nucleophosmin delocalization in thyroid tumour cellsAnnalisa Pianta, Cinzia Puppin, Nadia Passon, et al.
Hematological Oncology|July 14, 2009
Two novel NPM1 mutations in a therapy-responder AML patientAnnalisa Pianta, Dora Fabbro, Daniela Damiani, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|September 10, 2009
Unexpected phenotype of a typical NPM1 mutantAnnalisa Pianta, Dora Fabbro, Daniela Damiani, et al.
Endocrine|November 8, 2022
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structureAlessandra Franzoni, Federica Baldan, Nadia Passon, et al.
Neuropediatrics|October 10, 2017
Neurovisual Assessment in Children with Ataxia TelangiectasiaAlessandro Iodice, Jessica Galli, Anna Molinaro, et al.
Frontiers in Human Neuroscience|March 21, 2022
Age-Related Effects on the Spectrum of Cerebral Visual Impairment in Children With Cerebral PalsyJessica Galli, Erika Loi, Anna Molinaro, et al.
Clinical Case Reports|October 20, 2025
A Prenatal Diagnosis of Verheij Syndrome in a Fetus Harboring a de novo <i>PUF60</i> VariantCatia Mio, Maria Orsaria, Alessandra Franzoni, et al.
American Journal of Hematology|June 14, 2013
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patientsDaniela Damiani, Mario Tiribelli, Alessandra Franzoni, et al.
BMC Medical Genetics|October 15, 2015
A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosisPatrizia Dello Russo, Alessandra Franzoni, Federica Baldan, et al.
European Journal of Human Genetics : EJHG|November 12, 2020
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotypeCatia Mio, Lorenzo Allegri, Nadia Passon, et al.
Endocrine Pathology|January 25, 2011
Nucleophosmin delocalization in thyroid tumour cellsAnnalisa Pianta, Cinzia Puppin, Nadia Passon, et al.
Hematological Oncology|July 14, 2009
Two novel NPM1 mutations in a therapy-responder AML patientAnnalisa Pianta, Dora Fabbro, Daniela Damiani, et al.
Pageof 4